LOH SHUEN-HSING AND KYI ZU-YOONG, . CHEMOTHERAPEUTIC STUDIES ON SCHISTOSOMIASIS Ⅻ. SYNTHETIC STUDIES ON SOME PHOSPHORUS COMPOUNDSJ. Acta Pharmaceutica Sinica, 1963, 10(5): 293-297.
Citation: LOH SHUEN-HSING AND KYI ZU-YOONG, . CHEMOTHERAPEUTIC STUDIES ON SCHISTOSOMIASIS Ⅻ. SYNTHETIC STUDIES ON SOME PHOSPHORUS COMPOUNDSJ. Acta Pharmaceutica Sinica, 1963, 10(5): 293-297.

CHEMOTHERAPEUTIC STUDIES ON SCHISTOSOMIASIS Ⅻ. SYNTHETIC STUDIES ON SOME PHOSPHORUS COMPOUNDS

  • Condensation of N-chloroacetyl derivatives of several aromatic amines or aryl ureas with sodium O,O-dimethyl dithiophosphate gave the expected dithiophosphates carrying amide linkage. However, α-chloro-p-(chloro- or bromo)-acetanilide under similar conditions gave α,α'-dithio-bis-p-(chloro- or bromo)-acetanilide. Various phosphorylamides were prepared on condensation of substituted phenols, phosphorus oxychloride and substituted anilines in the presence of pyridine. Feebly basic 2,4,6-tribromoaniline failed to give aromatic phosphorylamides, but formed α-(2,4,6-tribromoanilino)-2,4,6-tribromoacetanilide on chloroacetylation.
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